An excellent role for Clinical Research Associate (CRA) to work for a Top 5 CRO based in Middlesex. My client is seeking CRAs with a minimum of 12 months CRA experience - independent monitoring in the UK.

Key responsibilities:

Undertake primary monitoring of sites participating in studies sponsored by my client in accordance with current ICH/GCP guidelines, local regulatory requirements and SOPs.
All site co-ordination activities will also be undertaken including drug accountability and data resolution and the CRA will assist the site in Ethics Committee submissions and preparation of informed consent forms.
The CRA will be responsible for the quality of the data for those sites to which he or she is assigned as monitor.

Education and qualification:

Life Sciences graduate (ideally)
12 months monitoring experience in the UK or EU.
Understanding of current ICH/GCP guidelines.
To apply for this position please send your CV to xxxxxxx.xxxxx@xxxxxxxxx.xxx / xxxx@xxxxxxxxx.xxx or call on 0115 935 2200.

It is unlawful to employ a person who does not have permission to live and work in the UK. Unless the advert states otherwise, please ensure you have this permission before applying.